Canonical Allele Identifier: CA2317593720

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226542_1226543delinsGC , CM000681.2:g.1226542_1226543delinsGC	GRCh38
NC_000019.9:g.1226541_1226542delinsGC , CM000681.1:g.1226541_1226542delinsGC	GRCh37
NC_000019.8:g.1177541_1177542delinsGC	NCBI36
NG_007460.2:g.42136_42137delinsGC , LRG_319:g.42136_42137delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2798_*2799delinsGC	ENSP00000490268.2:n.*2798_*2799delinsGC
ENST00000585748.3:c.825_826delinsGC	ENSP00000477641.2:p.Gln275=
ENST00000585851.2:c.1023_1024delinsGC	ENSP00000467912.2:p.Gln341=
ENST00000326873.12:c.1197_1198delinsGC MANE Select	ENSP00000324856.6:p.Gln399=
ENST00000326873.11:c.1197_1198delinsGC	ENSP00000324856.6:p.Gln399=
ENST00000585465.2:n.2930_2931delinsGC
ENST00000586243.5:c.1197_1198delinsGC	ENSP00000467240.2:p.Gln399=
ENST00000589152.5:n.1895_1896delinsGC
NM_000455.4:c.1197_1198delinsGC , LRG_319t1:c.1197_1198delinsGC	NP_000446.1:p.Gln399=
XM_005259617.1:c.1192_1193delinsGC	XP_005259674.1:p.Ala398=
XM_011528209.1:c.970_971delinsGC	XP_011526511.1:p.Ala324=
XM_005259617.3:c.1192_1193delinsGC	XP_005259674.1:p.Ala398=
XM_011528209.2:c.970_971delinsGC	XP_011526511.1:p.Ala324=
XR_001753738.2:n.2003_2004delinsGC
XR_001753740.2:n.1973_1974delinsGC
NM_000455.5:c.1197_1198delinsGC MANE Select	NP_000446.1:p.Gln399=